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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C51-412
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-65616
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C57-15
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-43
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-41
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-6561
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C57-15
filingDate 2019-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2021-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-110615814-B
titleOfInvention Preparation method of tenofovir disoproxil hemifumarate
abstract The invention provides a preparation method of tenofovir disoproxil hemifumarate. A method for preparing tenofovir disoproxil hemifumarate by a one-pot method. The generation of impurities in the synthesis process of tenofovir disoproxil is controlled by adding the water-binding agent, so that the intermediate tenofovir disoproxil is not required to be completely separated from a reaction system, the reaction treatment steps are saved, the loss in the process is reduced, and under the preferable process, the purity of the prepared tenofovir disoproxil hemifumarate is more than 99.0 percent, and the impurity tenofovir monofuroate is less than 0.1 percent; the total molar yield is stabilized at 77-85%.
priorityDate 2019-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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